Canonical Allele Identifier: CA3182815
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs761817133
gnomAD v2: 5-1213540-C-G
gnomAD v4: 5-1213425-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213425C>G , CM000667.2:g.1213425C>G GRCh38
NC_000005.9:g.1213540C>G , CM000667.1:g.1213540C>G GRCh37
NC_000005.8:g.1266540C>G NCBI36
NG_008282.1:g.16831C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.664-38C>G MANE Select ENSP00000305302.10:n.664-38C>G
ENST00000304460.10:c.664-38C>G ENSP00000305302.10:n.664-38C>G
ENST00000515652.5:c.572-38C>G ENSP00000425701.1:n.572-38C>G
NM_001003841.2:c.664-38C>G NP_001003841.1:n.664-38C>G
NM_001003841.3:c.664-38C>G MANE Select NP_001003841.1:n.664-38C>G